My CF Climb Story
Quinn the Mighty
On June 8, 2024, we welcomed our daughter Quinn into the world. Two weeks later, she was diagnosed with Cystic Fibrosis. Our journey has already been hard, with her case being more severe and already requiring hospitalization. But we are grateful for the support of our friends, family, and all the wonderful people at CHOP who have our daughter's back.
We are raising money for our first CF event on behalf of Quinn. Please consider donating to support her and the CF Foundation's efforts and research for new treatments. With your help, we can cure this disease in our daughter's lifetime. Please consider joining us and help make medical history.
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